scholarly journals Prospective risk assessments of patient safety events related to drug shortages in hospitals: Three actor-level perspectives

Author(s):  
Joo Hanne Poulsen ◽  
Marianne Hald Clemmensen ◽  
Lotte Stig Nørgaard ◽  
Peter Dieckmann
2021 ◽  
Author(s):  
Hoda Sabati ◽  
Amin Mohsenzadeh ◽  
Nooshin Khelghati

Patient safety is an aim for clinical applications and is a fundamental principle of healthcare and quality management. The main global health organizations have incorporated patient safety in their review of work practices. The data provided by the medical laboratories have a direct impact on patient safety and a fault in any of processes such as strategic, operational and support, could affect it. To provide appreciate and reliable data to the physicians, it is important to emphasize the need to design risk management plan in the laboratory. Failure Mode and Effect Analysis (FMEA) is an efficient technique for error detection and reduction. Technical Committee of the International Organization for Standardization (ISO) licensed a technical specification for medical laboratories suggesting FMEA as a method for prospective risk analysis of high-risk processes. FMEA model helps to identify quality failures, their effects and risks with their reduction/elimination, which depends on severity, probability and detection. Applying FMEA in clinical approaches can lead to a significant reduction of the risk priority number (RPN).


2019 ◽  
Vol 37 (3) ◽  
pp. 304-312 ◽  
Author(s):  
Ian H. Stanley ◽  
Skip Simpson ◽  
Hal S. Wortzel ◽  
Thomas E. Joiner

Health Policy ◽  
2018 ◽  
Vol 122 (12) ◽  
pp. 1302-1309 ◽  
Author(s):  
André Said ◽  
Ralf Goebel ◽  
Matthias Ganso ◽  
Petra Zagermann-Muncke ◽  
Martin Schulz

2011 ◽  
Vol 46 (12) ◽  
pp. 943-951 ◽  
Author(s):  
A. MacDonald Elyse ◽  
R. Fox Erin ◽  
S. Tyler Linda

2015 ◽  
Vol 38 (3) ◽  
pp. 205-208 ◽  
Author(s):  
Milena M. McLaughlin ◽  
Erik W. Skoglund

2013 ◽  
Vol 26 (3) ◽  
pp. 183-191 ◽  
Author(s):  
Anne Elise Rider ◽  
Derek J. Templet ◽  
Mitchell J. Daley ◽  
Carrie Shuman ◽  
Leticia V. Smith

Objective: The objectives of this article are to review the clinical implications of drug shortages highlighting patient safety, sedation, and oncology and introduce an expanded phase approach for the management of drug shortages. Data Sources: Literature retrieval was accessed through a PubMed search of English-language sources from January 1990 through April 2012 using the medical subject heading pharmaceutical preparations/supply and distribution and the general search term drug shortages. Study Selection and Data Extraction: All original prospective and retrospective studies, peer-reviewed guidelines, consensus statements, and review articles were evaluated for inclusion. Relevance was determined considering the therapeutic class, focus on drug shortages, and manuscript type. Data Synthesis: The increased number of drug shortages has created significant challenges for health care providers. Two particularly vulnerable populations are critically ill and oncology patients. A lack of therapeutic alternatives in critically ill patients may impact patient safety as well as treatment outcomes. Similarly, a chemotherapy agent in short supply may contribute to adverse outcomes in oncology patients. Conclusions: The mounting number of drug shortages has created a health care crisis, requiring changes in management strategies as well as clinical practice. The expanded phased approach outlined here provides a consistent, systematic approach for the management of drug shortages.


2013 ◽  
Vol 9 (3) ◽  
pp. 154-159 ◽  
Author(s):  
Monika C. Kerckhoffs ◽  
Alexander F. van der Sluijs ◽  
Jan M. Binnekade ◽  
Dave A. Dongelmans

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